Phase II evaluation of didemnin B in advanced adenocarcinoma of the kidney. A Southwest Oncology Group study

Invest New Drugs. 1992 Apr;10(1):55-6. doi: 10.1007/BF01275484.

Abstract

The Southwest Oncology Group studied the response rate and toxicity of didemnin B (3.47 mg/m2 i.v. q 28 days) in patients with advanced renal cell carcinoma. There were no responses in 22 response evaluable patients. Toxicity was significant with 10 patients having grade 3 or 4 toxicity. Toxicity seen included nausea and vomiting, exacerbation of coronary artery disease, hyperglycemia, anorexia, diarrhea and hepatitis. Didemnin B was toxic but inactive in patients with renal cell treated at this dose.

Publication types

  • Clinical Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenocarcinoma / drug therapy*
  • Adult
  • Aged
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / adverse effects
  • Depsipeptides*
  • Drug Evaluation
  • Female
  • Humans
  • Kidney Neoplasms / drug therapy*
  • Male
  • Middle Aged
  • Peptides, Cyclic / administration & dosage*
  • Peptides, Cyclic / adverse effects

Substances

  • Antineoplastic Agents
  • Depsipeptides
  • Peptides, Cyclic
  • didemnins